Variant #0000657768 (NC_000016.9:g.20975546T>C, NM_017539.1:c.9660A>G (DNAH3))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.20975546T>C
DNA change (hg38) g.20964224T>C
Published as DNAH3(NM_001347886.1):c.9522A>G (p.K3174=)
ISCN -
DB-ID DNAH3_000027
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-09 14:03:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH3 NM_017539.1 -?/. - c.9660A>G r.(?) p.(Lys3220=)
TMEM159 NM_020422.4 -?/. - c.-194727T>C r.(?) p.(=)


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